Canonical Allele Identifier: CA2209073367

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935623A= , CM000678.2:g.13935623A=	GRCh38
NC_000016.9:g.14029480A= , CM000678.1:g.14029480A=	GRCh37
NC_000016.8:g.13936981A=	NCBI36
NG_011442.1:g.20467A= , LRG_463:g.20467A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1769A=
ENST00000682617.1:c.1829A=	ENSP00000507912.1:p.Tyr610=
ENST00000682826.1:c.*1005A=	ENSP00000507274.1:n.*1005A=
ENST00000682909.1:n.3731A=
ENST00000683277.1:n.3336A=
ENST00000683407.1:n.1699A=
ENST00000683962.1:c.*1385A=	ENSP00000506854.1:n.*1385A=
ENST00000311895.8:c.1691A= MANE Select	ENSP00000310520.7:p.Tyr564=
ENST00000311895.7:c.1691A=	ENSP00000310520.7:p.Tyr564=
ENST00000389138.7:n.968A=
NM_005236.2:c.1691A= , LRG_463t1:c.1691A=	NP_005227.1:p.Tyr564=
XM_011522424.1:c.1829A=	XP_011520726.1:p.Tyr610=
XM_011522425.1:c.1148A=	XP_011520727.1:p.Tyr383=
XM_011522426.1:c.902A=	XP_011520728.1:p.Tyr301=
XM_011522427.1:c.341A=	XP_011520729.1:p.Tyr114=
XR_932805.1:n.1850A=
XM_011522424.3:c.1829A=	XP_011520726.1:p.Tyr610=
XM_017023043.2:c.902A=	XP_016878532.1:p.Tyr301=
NM_005236.3:c.1691A= MANE Select	NP_005227.1:p.Tyr564=